rs63749885
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
(C;T) | 9 | early-onset Alzheimers disease |
Make rs63749885(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 14 |
Position | 73186859 |
Gene | PSEN1 |
is a | snp |
is | mentioned by |
dbSNP | rs63749885 |
dbSNP (classic) | rs63749885 |
ClinGen | rs63749885 |
ebi | rs63749885 |
HLI | rs63749885 |
Exac | rs63749885 |
Gnomad | rs63749885 |
Varsome | rs63749885 |
LitVar | rs63749885 |
Map | rs63749885 |
PheGenI | rs63749885 |
Biobank | rs63749885 |
1000 genomes | rs63749885 |
hgdp | rs63749885 |
ensembl | rs63749885 |
geneview | rs63749885 |
scholar | rs63749885 |
rs63749885 | |
pharmgkb | rs63749885 |
gwascentral | rs63749885 |
openSNP | rs63749885 |
23andMe | rs63749885 |
SNPshot | rs63749885 |
SNPdbe | rs63749885 |
MSV3d | rs63749885 |
GWAS Ctlg | rs63749885 |
Max Magnitude | 9 |
rs63749885, also known as H163Y or His163Tyr, is a SNP in the presenilin 1 PSEN1 gene.
Inherited as an autosomal dominant, the rare rs63749885(T) allele is considered pathogenic for early-onset Alzheimer's disease.[PMID 7550536]
ClinVar | |
---|---|
Risk | rs63749885(T;T) |
Alt | rs63749885(T;T) |
Reference | Rs63749885(C;C) |
Significance | Pathogenic |
Disease | Alzheimer disease not provided |
Variation | info |
Gene | PSEN1 |
CLNDBN | Alzheimer disease, type 3 not provided |
Reversed | 0 |
HGVS | NC_000014.8:g.73653567C>T |
CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
CLNACC | RCV000019758.28, RCV000084317.1, |